HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255620G>C , CM000671.2:g.133255620G>C | GRCh38 |
NC_000009.11:g.136131007G>C , CM000671.1:g.136131007G>C | GRCh37 |
NC_000009.10:g.135120828G>C | NCBI36 |
NG_006669.1:g.22048C>G | |
NG_006669.2:g.24596C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.1140C>G | ||
ENST00000647353.1:n.54-4468C>G | ||
ENST00000679909.1:c.28+19542C>G | ENSP00000506089.1:n.28+19542C>G | |
ENST00000453660.3:n.1122C>G | ||
ENST00000538324.2:c.1104C>G | ENSP00000483018.1:p.Pro368= | |
ENST00000611156.4:c.*46C>G | ENSP00000483265.1:n.*46C>G | |
NM_020469.2:c.*46C>G | NP_065202.2:n.*46C>G | |
NM_020469.3:c.*46C>G | NP_065202.2:n.*46C>G |